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dc.creatorGeorgiadis N., Tsarouhas K., Rezaee R., Nepka H., Kass G.E.N., Dorne J.-L.C.M., Stagkos D., Toutouzas K., Spandidos D.A., Kouretas D., Tsitsimpikou C.en
dc.date.accessioned2023-01-31T07:40:41Z
dc.date.available2023-01-31T07:40:41Z
dc.date.issued2020
dc.identifier10.3892/or.2020.7688
dc.identifier.issn1021335X
dc.identifier.urihttp://hdl.handle.net/11615/72130
dc.description.abstractAnthracyclines are commonly used anticancer drugs with well.known and extensively studied cardiotoxic effects in humans. In the clinical setting guidelines for assessing cardiotoxicity are well.established with important therapeutic implications. Cardiotoxicity in terms of impairment of cardiac function is largely diagnosed by echocardiography and based on objective metrics of cardiac function. Until this day, cardiotoxicity is not an endpoint in the current general toxicology and safety pharmacology preclinical studies, although other classes of drugs apart from anthracyclines, along with everyday chemicals have been shown to manifest cardiotoxic properties. Also, in the relevant literature there are not well.established objective criteria or reference values in order to uniformly characterize cardiotoxic adverse effects in animal models. This in depth review focuses on the evaluation of two important echocardiographic indices, namely ejection fraction and fractional shortening, in the literature concerning anthracycline administration to rats as the reference laboratory animal model. The analysis of the gathered data gives promising results and solid prospects for both, defining anthracycline cardiotoxicity objective values and delineating the guidelines for assessing cardiotoxicity as a separate hazard class in animal preclinical studies for regulatory purposes. © 2020 Spandidos Publications. All rights reserved.en
dc.language.isoenen
dc.sourceOncology Reportsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85088513003&doi=10.3892%2for.2020.7688&partnerID=40&md5=ea28343656475a14e85c43c0cf88608a
dc.subjectanthracyclineen
dc.subjectdaunorubicinen
dc.subjectdoxorubicinen
dc.subjectepirubicinen
dc.subjectanthracyclineen
dc.subjectantineoplastic antibioticen
dc.subjectageen
dc.subjectalcohol consumptionen
dc.subjectArticleen
dc.subjectcardiotoxicityen
dc.subjectcardiovascular risken
dc.subjectcongestive heart failureen
dc.subjectdisease associationen
dc.subjectdrug safetyen
dc.subjectechocardiographyen
dc.subjectfractional shorteningen
dc.subjectheart left ventricle contractilityen
dc.subjectheart left ventricle ejection fractionen
dc.subjectheart left ventricle enddiastolic diameteren
dc.subjectheart left ventricle enddiastolic volumeen
dc.subjectheart left ventricle endsystolic diameteren
dc.subjectheart left ventricle endsystolic volumeen
dc.subjectheart muscle contractilityen
dc.subjecthypercholesterolemiaen
dc.subjecthypertensionen
dc.subjectimage analysisen
dc.subjectnonhumanen
dc.subjectobesityen
dc.subjectphysical inactivityen
dc.subjectpriority journalen
dc.subjecttobacco useen
dc.subjectanimalen
dc.subjectanimal modelen
dc.subjectcardiotoxicityen
dc.subjectpractice guidelineen
dc.subjectproceduresen
dc.subjectraten
dc.subjecttoxicity testingen
dc.subjectAnimalsen
dc.subjectAnthracyclinesen
dc.subjectAntibiotics, Antineoplasticen
dc.subjectCardiotoxicityen
dc.subjectEchocardiographyen
dc.subjectGuidelines as Topicen
dc.subjectModels, Animalen
dc.subjectRatsen
dc.subjectToxicity Testsen
dc.subjectSpandidos Publicationsen
dc.titleWhat is considered cardiotoxicity of anthracyclines in animal studiesen
dc.typejournalArticleen


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